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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Acute Toxicity: other routes

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Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
other information
Study period:
1967
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study meets generally accepted scientific principles. Study acceptable for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1967

Materials and methods

Principles of method if other than guideline:
no guideline reported
single i.p. application to mouse, observation period 2 weeks
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-chlorobenzothiazole
EC Number:
210-415-0
EC Name:
2-chlorobenzothiazole
Cas Number:
615-20-3
Molecular formula:
C7H4ClNS
IUPAC Name:
2-chloro-1,3-benzothiazole
Details on test material:
no purity specified

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
no further details reported

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
corn oil
Details on exposure:
undiluted 2-Chlorobenzothiazole or 10 % w/v in corn oil
Doses:
10, 50, 100, 3200 mg/kg bw
No. of animals per sex per dose:
2 + 2 (16 animals in total)
Control animals:
not specified
Details on study design:
single application, observation period 14 d

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
50 - 100 mg/kg bw
Based on:
test mat.
Remarks on result:
other: time of death 2 h - 2 d
Mortality:
at highest dose time to death = 2h
Clinical signs:
quite to very weak:
- rough fur
- vasoconstriction and/or cyanosis
Body weight:
increased during observation period
Gross pathology:
histopathological examination:
- chronic pneumonitis (in 10 mg/kg bw and 50 mg/kg bw groups)
- focal chronic interstititial nephritis ( in 1 out of 2 animals of the 10 mg/kg bw group)
- hydronephrosis ( in 1 out of 2 animals of the 3200 mg/kg bw group)(details not given)
- mild degree of hemosiderosis of the liver ( in 2 out of 2 animals of the 10 mg/kg bw group)
- moderately to severe liver necrosis ( in 2 out of 2 animals of the 3200 mg/kg bw group)

Applicant's summary and conclusion

Conclusions:
The LD50 (rat) is 50 - 100 mg/kg bw, applied i.p.